Evidence map›Paper›PMID 41090063›Full record

ReviewActa ortopedica brasileira2025

ROLE OF POLYMORPHISMS IN VEGF AND KDR GENES IN OSTEOSARCOMA SUSCEPTIBILITY: A SYSTEMATIC REVIEW.

Amanda Dos Santos Cavalcanti, Jéssica Vilarinho Cardoso, Verônica Aran Ponte, Jade Pires Nascimento, Mariana Chantre-Justino, Ana Cristina DE Sá Lopes, Walter Meohas, Jamila Alessandra Perini

Abstract readReview
In one paragraph

Review in Acta ortopedica brasileira, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Amanda Dos Santos Cavalcanti. Instituto Nacional de Traumatologia e Ortopedia (INTO), Divisao de Pesquisa, Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0002-8792-7524
Jéssica Vilarinho Cardoso. Universidade do Estado do Rio de Janeiro (UERJ), Laboratorio de Pesquisa em Ciencias Farmaceuticas (LAPESF), Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0002-6758-3664
Verônica Aran Ponte. Instituto Estadual do Cerebro Paulo Niemeyer, Laboratorio de Biomedicina do Cerebro, Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0003-2751-0986
Jade Pires Nascimento. Universidade do Estado do Rio de Janeiro (UERJ), Laboratorio de Pesquisa em Ciencias Farmaceuticas (LAPESF), Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0009-0001-2667-5386
Mariana Chantre-Justino. Instituto Nacional de Traumatologia e Ortopedia (INTO), Divisao de Pesquisa, Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0002-7351-5588
Ana Cristina DE Sá Lopes. Instituto Nacional de Traumatologia e Ortopedia (INTO), Divisao de Pesquisa, Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0009-0008-9922-2389
Walter Meohas. Instituto Nacional de Traumatologia e Ortopedia (INTO), Divisao de Pesquisa, Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0003-1402-9667
Jamila Alessandra Perini. Universidade do Estado do Rio de Janeiro (UERJ), Laboratorio de Pesquisa em Ciencias Farmaceuticas (LAPESF), Rio de Janeiro, RJ, Brazil.ORCID https://orcid.org/0000-0002-7683-0698

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is the most common aggressive primary bone tumor in children and adolescents. Angiogenesis, induced by vascular endothelial growth factor (VEGF) and its receptor (kinase insert domain receptor - KDR) is involved in tumor development. Both genes (VEGF and KDR) are polymorphic, and their association with osteosarcoma remains unclear. A systematic review of observational studies was performed to evaluate the association between polymorphisms in these genes and osteosarcoma development. Pubmed, Medline, Lilacs, and Scielo databases were searched for observational studies published up to April 2024. Eight publications of case-control studies were included, with quality ranging from 82% to 95%. All subjects were from the Chinese population: 1,681 cases and 2,049 controls. A total of six VEGF polymorphisms were analyzed. For osteosarcoma susceptibility, three studies found an increased risk with VEGF rs699947, four with VEGF rs2010963, two with VEGF rs3025039, one with VEGF rs833061, and no studies found an association with the VEGF rs1570360 and VEGF rs10434 SNPs. In addition, no studies evaluated SNPs in the KDR gene and osteosarcoma susceptibility. Further studies in diverse populations, particularly in Brazil, are necessary to clarify the role of VEGF and KDR polymorphisms in osteosarcoma development and prognosis. Level of evidence III; Systematic Review.

Indexed as

AngiogenesisGenetic PolymorphismOsteosarcomaSystematic ReviewVEGF

Identifiers

PMID41090063
PMCPMC12517555

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.